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Table of Contents
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For updated information on the status of ProHeart 6 please see FDA news - FDA Announces Limited Return of Heartworm Drug to U.S. Market
These pages contain safety information on products regulated by the FDA Center for Veterinary Medicine (CVM) and other FDA components.
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"Dear Doctor" Letters
Letters issued to veterinary medicine professionals by drug manufacturers alerting the professionals to important safety information.
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ProHeart®6, Fort Dodge Animal Health, June 5, 2008
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ProHeart®6 (moxidectin), Fort Dodge Animal Health, September 13, 2004 | pdf | (For updated information on the status of ProHeart 6 please see FDA news - FDA Announces Limited Return of Heartworm Drug to U.S. Market)
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Deramaxx, Novartis Animal Health US, December 22, 2003
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ProHeart®6, Fort Dodge Animal Health, June 19, 2003 | pdf |
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ProHeart®6, Fort Dodge Animal Health, July 22, 2002 | pdf |
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Baytril®, Bayer Corporation, July 6, 2000 | pdf |
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EtoGesic®, Tablets, Fort Dodge Animal Health, May 23, 2000 | pdf |
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RIMADYL®, Pfizer, Inc., March 9, 2000 | pdf |
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FDA Enforcement Report Index (Recalls and Legal Actions)
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The FDA Enforcement Report is published weekly by the Food and Drug Administration, U.S. Public Health Service, Department of Health and Human Services. It contains information on actions taken in connection with agency regulatory activities, including all FDA-classified recalls.
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FDA's Product Recalls, Alerts, and Warnings
Recalls are actions taken by a firm to remove a product from the market. Recalls may be conducted on a firm's own initiative, by FDA request, or by FDA order under statutory authority.
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How to Report an Adverse Drug Reaction
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MedWatch
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Recalls.gov
To provide better service in alerting the American people to unsafe, hazardous or defective products, six federal agencies with vastly different jurisdictions have joined together to create www.recalls.gov -- a "one stop shop" for U.S. Government recalls.
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EPA, Counterfeit Pesticide Products for Dogs and Cats
Web Page Updated by hd - June 18, 2008, 11:00 AM ET
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